Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsbg2 |
C |
A |
17: 57,152,443 (GRCm39) |
L666F |
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,588,344 (GRCm39) |
V4414E |
possibly damaging |
Het |
Apoc3 |
T |
G |
9: 46,144,585 (GRCm39) |
D79A |
probably damaging |
Het |
Arfgap1 |
T |
A |
2: 180,621,022 (GRCm39) |
|
probably null |
Het |
Ascc1 |
T |
C |
10: 59,843,551 (GRCm39) |
S38P |
probably benign |
Het |
Asl |
C |
T |
5: 130,040,791 (GRCm39) |
E389K |
probably benign |
Het |
Atat1 |
A |
T |
17: 36,215,008 (GRCm39) |
I215K |
probably benign |
Het |
Bod1l |
A |
T |
5: 41,991,075 (GRCm39) |
L160* |
probably null |
Het |
Cbl |
C |
A |
9: 44,069,836 (GRCm39) |
S637I |
possibly damaging |
Het |
Ccdc112 |
A |
C |
18: 46,420,720 (GRCm39) |
S343R |
probably benign |
Het |
Cr1l |
A |
G |
1: 194,799,925 (GRCm39) |
S250P |
possibly damaging |
Het |
Cspg4b |
T |
A |
13: 113,456,263 (GRCm39) |
F770I |
|
Het |
Dlgap3 |
A |
G |
4: 127,129,947 (GRCm39) |
E907G |
probably damaging |
Het |
Dsp |
A |
T |
13: 38,352,600 (GRCm39) |
E159D |
probably benign |
Het |
Ech1 |
G |
A |
7: 28,524,728 (GRCm39) |
|
probably benign |
Het |
Erbin |
G |
T |
13: 103,971,485 (GRCm39) |
N710K |
possibly damaging |
Het |
Fbxw28 |
A |
T |
9: 109,155,357 (GRCm39) |
|
probably null |
Het |
Gm4871 |
G |
C |
5: 144,969,012 (GRCm39) |
D100E |
probably damaging |
Het |
Got1l1 |
A |
G |
8: 27,687,619 (GRCm39) |
I388T |
probably damaging |
Het |
Ing5 |
T |
A |
1: 93,744,166 (GRCm39) |
N184K |
probably damaging |
Het |
Izumo3 |
A |
T |
4: 92,035,145 (GRCm39) |
L24* |
probably null |
Het |
Lig1 |
T |
C |
7: 13,020,491 (GRCm39) |
V99A |
possibly damaging |
Het |
Mbtps1 |
A |
G |
8: 120,255,794 (GRCm39) |
Y488H |
possibly damaging |
Het |
Muc5ac |
A |
G |
7: 141,358,520 (GRCm39) |
Y1240C |
possibly damaging |
Het |
Nav3 |
T |
C |
10: 109,594,828 (GRCm39) |
T1458A |
probably damaging |
Het |
Nedd1 |
T |
C |
10: 92,527,778 (GRCm39) |
E472G |
probably damaging |
Het |
Nod2 |
A |
T |
8: 89,391,685 (GRCm39) |
H664L |
possibly damaging |
Het |
Ntrk3 |
A |
G |
7: 78,227,450 (GRCm39) |
S28P |
probably damaging |
Het |
Or14a257 |
A |
G |
7: 86,138,231 (GRCm39) |
F176S |
probably damaging |
Het |
Or1i2 |
C |
T |
10: 78,448,242 (GRCm39) |
V78I |
probably benign |
Het |
Or2ag17 |
T |
A |
7: 106,390,338 (GRCm39) |
|
probably benign |
Het |
Or2ag17 |
C |
A |
7: 106,390,337 (GRCm39) |
|
probably benign |
Het |
Or6c66b |
T |
A |
10: 129,376,826 (GRCm39) |
M140K |
probably benign |
Het |
Pcdha4 |
G |
T |
18: 37,087,106 (GRCm39) |
G430W |
probably damaging |
Het |
Pcnx1 |
T |
A |
12: 82,030,385 (GRCm39) |
Y1114* |
probably null |
Het |
Pde6a |
T |
A |
18: 61,364,566 (GRCm39) |
D207E |
probably damaging |
Het |
Plekhg1 |
T |
A |
10: 3,902,326 (GRCm39) |
I540N |
|
Het |
Pnp2 |
A |
T |
14: 51,197,099 (GRCm39) |
I62F |
probably benign |
Het |
Rarg |
C |
A |
15: 102,148,334 (GRCm39) |
D258Y |
probably damaging |
Het |
Rnps1 |
T |
A |
17: 24,643,484 (GRCm39) |
M262K |
unknown |
Het |
Scaf11 |
T |
C |
15: 96,316,483 (GRCm39) |
D1027G |
probably benign |
Het |
Serpina3a |
A |
T |
12: 104,079,110 (GRCm39) |
|
probably benign |
Het |
Slc25a1 |
A |
G |
16: 17,744,297 (GRCm39) |
|
probably null |
Het |
Slc44a3 |
A |
C |
3: 121,291,521 (GRCm39) |
V365G |
probably benign |
Het |
Slc9a2 |
T |
A |
1: 40,757,809 (GRCm39) |
I116K |
probably damaging |
Het |
Stk36 |
T |
A |
1: 74,665,756 (GRCm39) |
S700T |
probably benign |
Het |
Tekt3 |
A |
G |
11: 62,968,945 (GRCm39) |
D224G |
probably benign |
Het |
Tgtp1 |
A |
T |
11: 48,877,841 (GRCm39) |
I288N |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,710,567 (GRCm39) |
V8485M |
unknown |
Het |
Tubg1 |
G |
T |
11: 101,014,854 (GRCm39) |
A199S |
probably benign |
Het |
Uso1 |
T |
A |
5: 92,306,280 (GRCm39) |
I79K |
probably damaging |
Het |
Utp20 |
C |
T |
10: 88,593,766 (GRCm39) |
D2215N |
probably damaging |
Het |
Wdr43 |
C |
T |
17: 71,923,350 (GRCm39) |
A32V |
probably benign |
Het |
Zfp704 |
T |
C |
3: 9,630,301 (GRCm39) |
D170G |
probably benign |
Het |
|
Other mutations in Slc45a3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00962:Slc45a3
|
APN |
1 |
131,905,265 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01626:Slc45a3
|
APN |
1 |
131,906,725 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01677:Slc45a3
|
APN |
1 |
131,906,708 (GRCm39) |
missense |
probably damaging |
0.99 |
F6893:Slc45a3
|
UTSW |
1 |
131,909,075 (GRCm39) |
missense |
probably benign |
|
R0122:Slc45a3
|
UTSW |
1 |
131,905,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R0402:Slc45a3
|
UTSW |
1 |
131,905,265 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1596:Slc45a3
|
UTSW |
1 |
131,909,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R1647:Slc45a3
|
UTSW |
1 |
131,905,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R1752:Slc45a3
|
UTSW |
1 |
131,905,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R1771:Slc45a3
|
UTSW |
1 |
131,904,694 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1776:Slc45a3
|
UTSW |
1 |
131,904,694 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2071:Slc45a3
|
UTSW |
1 |
131,905,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R2939:Slc45a3
|
UTSW |
1 |
131,905,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R4230:Slc45a3
|
UTSW |
1 |
131,909,399 (GRCm39) |
missense |
probably damaging |
0.96 |
R4876:Slc45a3
|
UTSW |
1 |
131,909,285 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4906:Slc45a3
|
UTSW |
1 |
131,909,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R5265:Slc45a3
|
UTSW |
1 |
131,905,932 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5964:Slc45a3
|
UTSW |
1 |
131,905,811 (GRCm39) |
missense |
probably damaging |
0.98 |
R6849:Slc45a3
|
UTSW |
1 |
131,905,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R7483:Slc45a3
|
UTSW |
1 |
131,904,549 (GRCm39) |
start gained |
probably benign |
|
R8322:Slc45a3
|
UTSW |
1 |
131,905,523 (GRCm39) |
missense |
probably damaging |
0.99 |
R8333:Slc45a3
|
UTSW |
1 |
131,905,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R9011:Slc45a3
|
UTSW |
1 |
131,905,714 (GRCm39) |
missense |
probably benign |
0.02 |
R9035:Slc45a3
|
UTSW |
1 |
131,909,187 (GRCm39) |
frame shift |
probably null |
|
R9101:Slc45a3
|
UTSW |
1 |
131,905,175 (GRCm39) |
missense |
possibly damaging |
0.51 |
|